Reficio DBM Plus

GUDID 00888480588559

EBI, LLC

Bone matrix implant, human-derived

• Primary Device ID: 00888480588559
• NIH Device Record Key: 3ba3014e-b7a8-4d0f-ac42-16209095a965
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reficio DBM Plus
• Version Model Number: 20800521
• Company DUNS: 050410323
• Company Name: EBI, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: true
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00888480588559 [Primary]

FDA Product Code

• MBP: Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-10-19

On-Brand Devices [Reficio DBM Plus]

• 00888480588580: 20900521
• 00888480588573: 20900421
• 00888480588566: 20900321
• 00888480588559: 20800521